Antibacterial composition for combating carbapenem-resistant gram-negative bacteria comprising adk protein as active ingredient

ABSTRACT

Provided is an antibacterial composition against carbapenem-resistant gram-negative bacteria which includes, as an active ingredient, adenylate kinase (ADK) protein derived from  Mycobacterium tuberculosis . The ADK protein derived from  Mycobacterium tuberculosis , according to the subject matter, has excellent antimicrobial activity against carbapenem-resistant gram-negative bacteria, and thus may be usefully used in a variety of fields as an antibacterial composition.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to and the benefit of Korean Patent Application No. 10-2015-0047360 filed on Apr. 3, 2015 and International Patent Application No. PCT/KR2016/003467, filed on Apr. 4, 2016, the disclosure of which is incorporated herein by reference in its entirety.

STATEMENT REGARDING GOVERNMENT RIGHTS

The present invention was undertaken with the support of 1) Functional analysis of PADK as therapeutic drugs for Polymicrobial sepsis and Carbapenem-resistance Gram-negative bacterial sepsis No. 2015R1A2A1A13001713 grant funded by the National Research Foundation of Korea, 2) Laboratory of Integrated Immunoregulation (LII) No. 2013R1A4A1069575 grant funded by the National Research Foundation of Korea.

SEQUENCE LISTING

The Sequence Listing submitted in text format (.txt) filed on Oct. 2, 2017, named “SequenceListing.txt”, created on Sep. 22, 2017, 3.00 KB), is incorporated herein by reference.

TECHNICAL FIELD

The present invention relates to an antibacterial composition against carbapenem-resistant gram-negative bacteria which includes, as an active ingredient, adenylate kinase (ADK) protein derived from Mycobacterium tuberculosis.

BACKGROUND ART

Generally, antibacterial agents collectively refer to antimicrobial agents, in particular, substances having an antimicrobial effect, in particular, substances having an excellent antimicrobial effect through inhibition of systems in which bacteria synthesize cell walls, proteins, or the like, or agents prepared therefrom. Major ingredients of antibacterial agents are extracted mainly from fungi, and such antibacterial agents are widely used these days to treat diseases caused by bacterial infection, and the like.

Starting with the discovery of penicillin antibiotics by Fleming in the 20^(th) century, numerous antimicrobial agents and antibiotics have been developed to escape from diseases caused by bacterial infections. Such antibacterial agents occupy an essential position in our lives, and are widely used in a variety of applications such as drugs, foods, cosmetic preservatives, and the like. However, in the case of antibacterial agents using chemical synthetic materials, the number of bacteria having resistance thereto gradually increases, and, accordingly, the use thereof is increasingly limited.

Antimicrobial-resistant bacteria refer to bacteria that are resistant to certain antimicrobial agents and thus do not respond thereto. For example, penicillin-resistant Staphylococcus aureus that does not respond to penicillin belongs to these bacteria. In addition, methicillin-resistant Staphylococcus aureus (MRSA), which was first reported in the academic world in 1961 and since then, has become a major pathogenic infectious bacterium globally, and vancomycin resistant enterococcus (VRE), which has resistance to vancomycin, first discovered in Europe in 1988, are known, and in the late 1990s, vancomycin intermediate-resistant staphylococcus aureus (VISA) was reported in Japan, the U.S.A., France, and Korea. In addition, vancomycin-resistant staphylococcus aureus (VRSA), wherein vancomycin is known as the last therapeutic agent of staphylococcus aureus which is the most common causative bacterium of human infection, was first reported globally in 2002 by the Centers for Disease Control, and thus the possibility of proliferation of so-called super bacteria is greatly increasing.

Meanwhile, β-lactam antibiotics, considered most importantly in the antibiotics field, include penam antibiotics commonly known as penicillin, cefem antibiotics commonly known as cephalosporin, penem antibiotics, and carbapenem antibiotics. Among these, examples of carbapenem antibiotics include imipenem, panipenem, meropenem, ertapenem, and the like, which are commercially available.

Therefore, the inventors of the present invention made an effort to develop of novel antimicrobial agents and, as a result, verified that adenylate kinase or adenosine kinase (ADK) protein derived from Mycobacterium tuberculosis exhibited excellent antimicrobial activity against carbapenem-resistant gram-negative bacteria, thus completing the present invention.

DISCLOSURE Technical Problem

An object of the present invention is to provide an antibacterial composition against carbapenem-resistant gram-negative bacteria which includes ADK protein as an active ingredient.

Another object of the present invention is to provide a composition for the prevention or treatment of infectious diseases caused by carbapenem-resistant gram-negative bacteria, the composition including ADK protein as an active ingredient.

Technical Solution

The prevent invention provides an antibacterial composition, a quasi-drug, a food additive, or a feed additive against carbapenem-resistant gram-negative bacteria which includes ADK protein as an active ingredient.

The present invention also provides a pharmaceutical composition or a food composition for the prevention or treatment of infectious diseases caused by carbapenem-resistant gram-negative bacteria, the composition including ADK protein as an active ingredient.

Advantageous Effects

According to the present invention, ADK protein derived from Mycobacterium tuberculosis has excellent antibacterial activity against carbapenem-resistant gram-negative bacteria, and thus may be usefully used in a variety of fields as an antibacterial composition.

DESCRIPTION OF DRAWINGS

The FIGURE is an image showing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis results of recombinant ADK protein.

BEST MODE

Hereinafter, the present invention will be described in more detail.

The present invention provides an antibacterial composition against carbapenem-resistant gram-negative bacteria which includes ADK protein as an active ingredient.

The term “antibacterial” or “antibacterial activity” as used herein refers to a property of resisting microorganisms such as bacteria or fungi, more particularly, refers to properties of antibiotics and the like which inhibit the growth or proliferation of bacteria.

The term “antibacterial composition” as used herein refers to a composition having the activity of inhibiting the growth and development of microorganisms such as bacteria or fungi, and may include all forms used in a variety of fields requiring antimicrobial effects, for example, drugs, quasi-drugs, food additives, feed additives, or the like. In particular, the antibacterial composition may be used in products directly associated with microorganisms, such as: antibiotics or contamination inhibitors in the medical field; foods for antiseptic or antimicrobial purposes; in agriculture for antimicrobial, bactericidal, or antiseptic purposes; cosmetics or daily supplies to inhibit dandruff, prevent athlete's foot, or inhibit the odor of the armpits, or for anti-acne purposes; and the like, or detergents for cleaning, detergents for washing dishes, or the like for antiseptic, antimicrobial, or bactericidal purposes, but the present invention is not limited to the above purposes.

The ADK protein of the present invention is derived from Mycobacterium tuberculosis, may preferably have an amino acid sequence represented by SEQ ID NO: 1, may be encoded by a base sequence represented by SEQ ID NO: 2, and includes functional equivalents of the ADK protein. The term “functional equivalents” as used herein refers to proteins that have sequence homology of at least 70%, preferably, at least 80%, more preferably, at least 90%, most preferably, at least 95% with the amino acid sequence of SEQ ID NO: 1 as a result of the addition, substitution or deletion of amino acids and exhibit substantially the same physiological activity as that of the protein having the amino acid sequence of SEQ ID NO: 1 or the protein encoded by the base sequence of SEQ ID NO: 2.

The ADK protein of the present invention includes both proteins having natural amino acid sequences thereof and amino acid sequence variants thereof. The variants of the ADK protein refer to proteins having different sequences by deletion, insertion, or non-conservative or conservative substitution of an ADK natural amino acid sequence and one or more amino acid residues, or a combination thereof. Amino acid exchange in proteins and peptides that does not overall alter the activity of molecules is known in the art. The ADK protein or the variants thereof may be naturally extracted or synthesized (Merrifield, J. Amer. Chem. Soc. 85:2149-2156, 1963) or may be prepared by gene recombination based on a DNA sequence (Sambrook et al, Molecular Cloning, Cold Spring Harbor Laboratory Press, New York, USA, 2^(nd) Edition, 1989).

The ADK protein of the present invention may be encoded by a base sequence of SEQ ID NO: 2, and variants capable of performing functionally the same action as that of the nucleotide are included within the scope of the present invention.

The term “gram-negative bacteria” as used herein refers to bacteria stained red by Gram staining and, generally, these bacteria have strong resistance to pigments and surfactants. The gram-negative bacteria of the present invention include all types of gram-negative bacteria containing endotoxins, and examples thereof include, but are not limited to, bacteria belonging to the genus Escherichia, the genus Pseudomonas, the genus Acinetobacter, the genus Salmonella, the genus Klebsiella, the genus Neisseria, the genus Enterobacter, the genus Shigella, the genus Moraxella, the genus Helicobacter, the genus Stenotrophomonas, the genus Bdellovibrio, and the genus Legionella. In particular, examples of these gram-negative bacteria include, but are not limited to, Escherichia coli, Pseudomonas aeruginosa, Pseudomonas fluorescens, Pseudomonas putida, Pseudomonas chlororaphis, Pseudomonas pertucinogena, Pseudomonas stutzeri, Pseudomonas syringae, Acinetobacter baumannii, Acinetobacter lwoffii, Acinetobacter calcoaceticus, Acinetobacter haemolyticus, Salmonella enterica, Salmonella bongori, Salmonella enteritidis, Salmonella typhimurium, Salmonella gallinarum, Salmonella pullorum, Salmonella mbandaka, Salmonella choleraesuls, Salmonella thompson, Salmonella infantis, Salmonella derby, Klebsiella pneumonia, Klebsiella granulomatis, Klebsiella oxytoca, Klebsiella terrigena, Neisseria gonorrhoeae, Neisseria meningitidis, Enterobacter aerogenes, Enterobacter cloacae, Shigella boydii, Shigella dysenteriae, Shigella flexneri, Shigella sonnei, Moraxella catarrhalis, Moraxella lacunata, Moraxella bovis, Helicobacter pylori, Helicobacter heilmannii, Helicobacter felis, Helicobacter mustelae, Helicobacter fenelliae, Helicobacter rappini, Helicobacter hepaticus, Helicobacter bilis, Helicobacter pullorum, Stenotrophomonas maltophilia, Stenotrophomonas nitritireducens, Bdellovibrio bacteriovorus, Legionella pneumophila, Legionella anisa, Legionella birminghamensis, Legionella bozemanii, Legionella cincinnatiensis, Legionella dumoffii, Legionella feeleii, Legionella gormanii, Legionella hackeliae, Legionella israelensis, Legionella jordanis, Legionella lansingensis, Legionella longbeachae, Legionella maceachernii, Legionella micdadei, Legionella oakridgensis, Legionella sainthelensi, Legionella tucsonensis, and Legionella wadsworthii.

The term “carbapenem” as used herein refers to one type of β-lactam antibiotic which has a structure represented by Formula 1 below:

wherein, in Formula 1, each of R₁ and R₂ is independently H, a C₁-C₁₀ alkyl, or a C₁-C₁₀ alkyl substituted with a hydroxyl group, and

R₃ is H, —O—R₄, or —S—R₄,

wherein R₄ is a N-substituted or C-substituted amine or pyrrolidine.

Examples of carbapenem antibiotics include, but are not limited to, imipenem, meropenem, ertapenem, doripenem, panipenem/betamipron, biapenem, razupenem, tebipenem, lenapenem, and tomopenem.

Structures of imipenem, panipenem, meropenem, ertapenem, and doripenem, which are representative carbapenem antibiotics, are shown in Formulae 2, 3, 4, 5, and 6, respectively:

The ADK protein derived from Mycobacterium tuberculosis, according to the present invention, has excellent antimicrobial activity against carbapenem-resistant gram-negative bacteria, and thus may be usefully used as an antibacterial composition in a variety of fields, i.e., quasi-drugs, food additives, feed additives, and the like.

The present invention also provides an antibacterial quasi-drug, an antibacterial food additive, or an antibacterial feed additive against carbapenem-resistant gram-negative bacteria which includes ADK protein as an active ingredient.

The present invention also provides a composition for the prevention or treatment of infectious diseases caused by carbapenem-resistant gram-negative bacteria which includes ADK protein as an active ingredient.

The composition includes a pharmaceutical composition or a food composition.

The present invention also provides a method of preventing or treating infectious diseases caused by carbapenem-resistant gram-negative bacteria, the method including administering ADK protein to an individual.

The ADK protein of the present invention selectively exhibits excellent antimicrobial activity against carbapenem-resistant gram-negative bacteria, and thus a composition including the same may be usefully used in the prevention or treatment of infectious diseases caused by carbapenem-resistant gram-negative bacteria.

The term “infectious diseases” as used herein refers to illnesses caused by disease-causing pathogenic microorganisms, such as viruses, bacteria, fungi, and parasites through propagation and intrusion into animals or humans, and refers to all infectious diseases caused by carbapenem-resistant gram-negative bacteria in accordance with the objects of the present invention. For example, the infectious diseases of the present invention may be respiratory diseases, gastrointestinal diseases, inflammatory diseases, and the like. In particular, examples of the infectious diseases include, but are not limited to, pneumonia, peritonitis, meningitis, wound infections, osteoarthritis, cholecystitis, urinary tract infections, cerebromeningitis, endocarditis, myocarditis, pericarditis, arthritis, pharyngitis, gonorrhea, bacillary dysentery, enteritis, conjunctivitis, gastritis, tympanitis, cystitis, lymphangitis, and septicemia.

The term “prevention” as used herein means all actions that inhibit infectious diseases or delay the onset thereof via administration of the composition. The term “treatment” as used herein means all actions that alleviate or beneficially change symptoms due to infectious diseases via administration of the composition.

The pharmaceutical composition of the present invention may further include a commonly used suitable carrier, excipient or diluent. Examples of the carrier, the excipient, or the diluent that may be included in the pharmaceutical composition of the present invention include, but are not limited to, lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, microcrystalline cellulose, polyvinylpyrrolidone, water, methyl hydroxybenzoate, propyl hydroxybenzoate, talc, magnesium stearate, and mineral oil.

The pharmaceutical composition of the present invention may be administered in oral or parenteral forms according to a general method, and is formulated using generally used diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents, surfactants, and the like. Solid preparations for oral administration include tablets, pills, powders, granules, capsules, and the like, and such solid preparations are formulated by mixing the composition with at least one excipient, e.g., starch, calcium carbonate, sucrose, lactose, gelatin, and the like. In addition to simple excipients, lubricants such as magnesium stearate and talc are also used. Examples of liquid preparations for oral administration include suspensions, liquids for internal use, emulsions, syrups, and the like, and these liquid preparations may include, in addition to simple commonly used diluents, such as water and liquid paraffin, various types of excipients, for example, a wetting agent, a sweetener, a flavoring agent, a preservative, and the like. Preparations for parenteral administration include an aqueous sterile solution, a non-aqueous solvent, a suspension, an emulsion, a freeze-dried preparation, and a suppository. Non-limiting examples of the non-aqueous solvent and the suspension include propylene glycol, polyethylene glycol, a vegetable oil such as olive oil, and an injectable ester such as ethyl oleate. Examples of suppository bases include Witepsol, Macrogol, Tween 61, cacao butter, laurin, glycerogelatin, and the like.

The term “administration” as used herein refers to supply of the pharmaceutical composition of the present invention to an individual by using an appropriate method.

A suitable dose of the pharmaceutical composition of the present invention may vary depending on conditions and body weights of patients, severity of disease, types of drugs, administration route, and administration time, but may be appropriately selected by those of ordinary skill in the art. To obtain desired effects, the pharmaceutical composition of the present invention may be administered in an amount of 0.001 mg/kg to 1000 mg/kg daily. The pharmaceutical composition may be administered once or multiple times a day. The dosage is not intended to limit the scope of the present invention in any way.

The pharmaceutical composition of the present invention may be administered to an individual via a variety of routes. All administration methods may be expected, for example, oral injection, rectal or intravenous injection, muscular injection, subcutaneous injection, intrauterine epidural injection, and intracerebroventricular injection. However, for oral administration, since a protein is digested, an oral composition may be formulated such that active ingredients are coated, or formulated to be protected from being decomposed in the stomach. The composition of the present invention may be administered preferably in the form of an injection.

The pharmaceutical composition according to the present invention may further include one or more known substances having antimicrobial activity in addition to the ADK protein.

In the present invention, the food composition may be preferably in the form of health functional foods.

In the present invention, the health functional food refers to a group of foods having added values provided by a physical, biochemical, or biotechnological method so that the corresponding food imparts or exhibits intended functions suitable for specific applications, or a processed food designed such that a composition of the food sufficiently imparts, in the body, body modulation functions regarding biological defense rhythm control, disease prevention and recovery, and the like.

The health functional food may include sitologically acceptable food supplement additives, and may further include suitable carriers, excipients, and diluents commonly used to prepare a health functional food.

When the food composition of the present invention is used as a food additive, the composition may be appropriately used alone or in combination with other foods or food ingredients according to a commonly used method. A mixing amount of active ingredients may be appropriately determined according to the purpose of use (prevention, health or medical treatment). In general, in preparation of foods or beverages, the composition of the present invention may be added in an amount of 15 wt % or less, preferably, 10 wt % or less, with respect to raw materials. However, when ingested for a long period of time for health and hygiene purposes or for health control purposes, the food composition may be included in an amount in or less than the above ranges of amounts. The composition has no problem in terms of safety, and thus may also be used in an amount in or greater than the above ranges of amounts.

In addition to the above-listed ingredients, the food composition of the present invention may include various nutritional supplements, vitamins, electrolytes, flavors, colorants, pectic acid and salts thereof, alginic acid and salts thereof, organic acids, a protective colloid thickener, a pH adjusting agent, a stabilizer, a preservative, glycerin, alcohols, a carbonating agent used in carbonated beverages, and the like. In addition, the food composition of the present invention may include flesh for the preparation of natural fruit juice, fruit juice beverages, and vegetable beverages. These ingredients may be used alone or in combination. The proportion of these additives is not very important, but the amounts of the additives are generally selected from 0.01 parts by weight to 0.1 parts by weight based on 100 parts by weight of the composition of the present invention.

Hereinafter, exemplary examples will be described to aid in understanding of the present invention. However, these examples are provided only to more easily understand the present invention and are not intended to limit the scope of the present invention.

Example 1. Cloning of Recombinant ADK (Rv0733)

The ADK (Rv0733) region was amplified by PCR using genomic DNA of Mycobacterium tuberculosis H37Rv (ATCC 27294) as a template (primer: 5′-CATATGAGAGTTTTGTTGCTGGGACCG-3′ (SEQ ID NO: 3) and 5′-AAGCTTCTTTCCCAGAGCCCGCAACGC-3′ (SEQ ID NO: 4)). The isolated PCR product was digested with NdeI and HindIII enzymes and inserted into the expression vector pET22b. E. coli BL21 transformed with the vector pET22b into which the ADK gene was inserted was cultured in an LB medium (containing 100 g/ml of ampicillin) at 37° C. for 12 hours. Subsequently, 1 mM isopropyl-D-thiogalactopyranoside (IPTG) was added thereto, followed by culturing for 6 hours, and the cells were lysed with a lysis buffer (containing 1M DTT, lysozyme, and PMSF). A recombinant protein was purified using nickel-nitrilotriacetic acid agarose (Ni-NTA, Invitrogen, Carlsbad, Calif., USA) in accordance with a method of the manufacturer. Finally, the purified recombinant ADK protein was identified by SDS-PAGE. The results thereof are illustrated in the FIGURE.

Example 2. Identification of Carbapenem-Resistant Gram-Negative Bacteria

Acinetobacter baumannii KUMC.2014.90 and KUMC.2014.91 strains were isolated from blood samples of patients of the Division of Infectious Diseases of Korea University. To identify the resistance of the strains to antibiotics, a VITEK II system, which is an automated device, was primarily used and, as a result, it was confirmed that the strains have resistance to all carbapenem-based antibiotics, i.e., imipenem, meropenem, ertapenem, and the like (confirmed results values of R>32). Secondarily, the resistance of the strains to imipenem and meropenem, which are carbapenem-based antibiotics, was reconfirmed using a liquid medium microdilution method (confirmed result values of greater than 128 μg/ml).

Experimental Example 1. Verify Antibacterial Activity of ADK Protein Against Carbapenem-Resistant Gram-Negative Bacteria

To verify the antibacterial activity of the recombinant ADK protein obtained in Example 1 against the carbapenem-resistant Acinetobacter baumannii (KUMC.2014.90 and KUMC.2014.91 strains) obtained in Example 2, Rezazurin assay was performed according to a conventionally known method to measure a minimum inhibitory concentration (MIC) and a minimum bactericidal concentration (MBC) for the carbapenem-resistant Acinetobacter baumannii strains. As a control, Acinetobacter baumannii, which is a normal strain, was used. Experimental results are shown in Table 1 below.

TABLE 1 MIC (μg/ml) Organisms and Testing MBC antimicrobial agent range 50% 80% (μg/ml) Acinetobacter baumannii Ampicillin 0.45~500 <31.3 <62.5 <62.5 Rukasyn 0.45~500 <1 <2 <3.9 Cravit 0.45~500 <0.5 <1 <1 Prepenem 0.45~500 <0.5 <1 <1 Adk 0.45~500 <3.9 <7.8 <7.8 Acinetobacter baumannii (KUMC.2014.90) Ampicillin 0.45~500 No effect No effect No effect Rukasyn 0.45~500 <15.6 <31.3 <31.3 Cravit 0.45~500 <7.8 <15.6 <15.6 Prepenem 0.45~500 <31.3 <62.5 <62.5 Adk 0.45~500 <1 <2 <2 Acinetobacter baumannii (KUMC.2014.91) Ampicillin 0.45~500 No effect No effect No effect Rukasyn 0.45~500 <15.6 <31.3 <31.3 Cravit 0.45~500 <7.8 <15.6 <15.6 Prepenem 0.45~500 <31.3 <62.5 <62.5 Adk 0.45~500 <3.9 <7.8 <7.8

As shown in Table 1, as a result of calculating 50% and 80% inhibitory concentrations assuming that result values of wells not treated with antibiotics and ADK protein were 100%, it was confirmed that antibiotics (i.e., ampicillin, rukasyn, cravit, and prepenem) inhibited the growth of Acinetobacter baumannii, which is a normal strain, while being unable to inhibit the growth of the carbapenem-resistant Acinetobacter baumannii (KUMC.2014.90 and KUMC.2014.91 strains). In contrast, it was confirmed that the ADK protein significantly inhibited the growth of both Acinetobacter baumannii, which is a normal strain, and the two types of carbapenem-resistant Acinetobacter baumannii (KUMC.2014.90 and KUMC.2014.91 strains).

From the above-described experimental results, it was confirmed that ADK protein derived from Mycobacterium tuberculosis, according to the present invention, had excellent antimicrobial activity against carbapenem-resistant gram-negative bacteria.

Hereinafter, the pharmaceutical composition and food composition of the present invention will be described with reference to the following preparation examples. However, these examples are provided only for illustrative purposes and are not intended to limit the scope of the present invention.

Preparation Example 1. Preparation of Pharmaceutical Composition

1-1. Preparation of Powder

ADK protein 2 g Lactose 1 g

The above ingredients were mixed and airtight packages were filled therewith, thereby completing the preparation of powder.

1-2. Preparation of Tablets

ADK protein 100 mg Corn starch 100 mg Lactose 100 mg Magnesium stearate  2 mg

The above ingredients were mixed, and then tablets were prepared according to a general method of preparing tablets.

1-3. Preparation of Capsules

ADK protein 100 mg Corn starch 100 mg Lactose 100 mg Magnesium stearate  2 mg

The above ingredients were mixed, and then gelatin capsules were filled therewith according to a general method of preparing capsules, thereby completing the preparation of capsules.

Preparation Example 2. Preparation of Food Composition

2-1. Preparation of Health Food

ADK protein 100 mg Vitamin mixture appropriate amount Vitamin A acetate 70 g Vitamin E 1.0 mg Vitamin B1 0.13 mg Vitamin B2 0.15 mg Vitamin B6 0.5 mg Vitamin B12 0.2 g Vitamin C 10 mg Biotin 10 g Nicotinamide 1.7 mg Folic acid 50 g Calcium pantothenate 0.5 mg Mineral mixture appropriate amount Ferrous sulfate 1.75 mg Zinc oxide 0.82 mg Magnesium carbonate 25.3 mg Monopotassium phosphate 15 mg Dicalcium phosphate 55 mg Potassium citrate 90 mg Calcium carbonate 100 mg Magnesium chloride 24.8 mg

The vitamin mixture and the mineral mixture were composed of a mixture of relatively suitable ingredients for health foods as an exemplary embodiment, but the mixing ratio may be arbitrarily modified, and the above ingredients were mixed according to a general method of preparing health foods and prepared into granules, and may be used in the preparation of a health food composition according to a general method. 

1. An antibacterial composition against carbapenem-resistant gram-negative bacteria, the antibacterial composition comprising adenylate kinase (ADK) protein as an active ingredient.
 2. The antibacterial composition of claim 1, wherein the ADK protein is derived from Mycobacterium tuberculosis.
 3. The antibacterial composition of claim 1, wherein the ADK protein is represented by SEQ ID NO:
 1. 4. The antibacterial composition of claim 1, wherein the ADK protein is encoded by a base sequence represented by SEQ ID NO:
 2. 5. The antibacterial composition of claim 1, wherein the composition is an antibacterial quasi-drug composition.
 6. The antibacterial composition of claim 1, wherein the composition is an antibacterial food additive composition.
 7. The antibacterial composition of claim 1, wherein the composition is an antibacterial feed additive composition.
 8. The antibacterial composition of claim 1, wherein the composition is a pharmaceutical composition.
 9. The antibacterial composition of claim 1, wherein the composition is a food composition.
 10. A method of treating an infectious disease comprising administering the pharmaceutical composition of claim 8 to a subject in need thereof.
 11. A method of alleviating an infectious disease comprising administering the food composition of claim 9 to a subject in need thereof. 